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Fenbendazole

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
Fenbendazole
Clinical data
AHFS/Drugs.comInternational Drug Names
License data
ATC code
Identifiers
  • Methyl N-(6-phenylsulfanyl-1H-benzoimidazol-2-yl)carbamate
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.051.024Edit this at Wikidata
Chemical and physical data
FormulaC15H13N3O2S
Molar mass299.35 g·mol−1
3D model (JSmol)
  • COC(=O)Nc3nc2ccc(Sc1ccccc1)cc2[nH]3
  • InChI=1S/C15H13N3O2S/c1-20-15(19)18-14-16-12-8-7-11(9-13(12)17-14)21-10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19) checkY
  • Key:HDDSHPAODJUKPD-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Fenbendazole is a broad-spectrumbenzimidazoleanthelmintic used against gastrointestinal parasites including:roundworms,hookworms,whipworms, thetapeworm genusTaenia (but not effective againstDipylidium caninum, a common dog tapeworm),pinworms,Aelurostrongylus spp.,paragonimiasis,strongyles, andstrongyloides that can be administered tosheep,cattle,horses,fish,dogs,cats,rabbits, most reptiles, freshwater shrimp tanks asplanaria and hydra treatments, andseals.

It has not been tested or approved for use in humans by theFDA orEMA.[1] Related benzimidazole drugs such asmebendazole andalbendazole are used in humans.

Some laboratory research has shown promising results for fenbendazole and mebendazole asanticancer drugs. Exaggerated information has circulated on social media promoting fenbendazole as a miracle cancer cure. However, the possible use of fenbendazole against cancer is still at the stage of very early laboratory research, and should not be attempted without a doctor's approval and supervision. Misuse of fenbendazole can cause liver damage.

Mechanism of action

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Fenbendazole works by binding totubulin, a protein that is part of themicrotubules in the cells of parasites. This binding disrupts the microtubules' formation[2] and function, leading to the parasites' inability to absorb nutrients, resulting in their eventual death. This mode of action makes fenbendazole effective against both adult and larval stages of many parasitic worms.[3][4]

Uses in veterinary medicine

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Dogs and cats

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Fenbendazole is commonly used to treat intestinal parasites, including roundworms, hookworms, whipworms, and certain tapeworms. It is often administered as part of a broader deworming protocol.[5]

Horses

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In equine medicine, fenbendazole is used to control strongyles, pinworms, and ascarids. It is available in paste form for easy administration.[6]

Cattle and goats

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Fenbendazole is effective against lungworms, stomach worms, and intestinal worms in ruminants. It is administered through feed, drenching, or bolus form.[7]

Drug interactions

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Drug interactions may occur ifsalicylanilides such as dibromsalan andniclosamide are co-administered. Abortions in cattle and death in sheep have been reported after using these medications together.[8] Abortions in domestic ruminants have been associated with concurrent use of antitrematode therapeutic agents.[9]

Toxicity

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Fenbendazole is poorly absorbed from the gastrointestinal tract in most species. TheLD50 in laboratory animals exceeds 10 g/kg when administered orally.[8]

Metabolism

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Fenbendazole ismetabolized in the liver tooxfendazole, which is anthelmintic, too; oxfendazole partially gets reduced back to fenbendazole in the liver andrumen.[10][11] Also, fenbendazole itself is an active metabolite of another anthelmintic drug,febantel.[12]

Safety and precautions

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Fenbendazole is generally safe when used as directed, but following veterinary guidelines and dosage instructions to avoid potential side effects is important. Some animals may experience mild gastrointestinal upset. It is not recommended for use in pregnant animals without veterinary advice.[13] In treatment in dogs that go on for longer than the label recommendation, there have been reports of bone marrow hypoplasia and pancytopenia occurring.[14]

Two case reports describe dangerous liver injury in human patients taking fenbendazole off-label. When they stopped taking the drug, the liver injury resolved.[15][16]

Research directions

[edit]

Fenbendazole has been proposed forrepurposing as ananticancer drug due to its ability to disrupt energy metabolism in cancer cells and induce cell death through multiple mechanisms. Early results with fenbendazole and the related drugmebendazole are somewhat promising, fromin vitro studies, animal studies and a few case reports from people who took it off-label. Fenbendazole's poorbioavailability when administered orally, though, remains a challenge for its use as a cancer treatment. Some patients taking fenbendazole off-label without a doctor's supervision suffered potentially dangerous liver dysfunction, although this resolved after stopping taking the drug.[17][18][19]

Exaggerated reports have circulated on social media that fenbendazole is a "miracle cure" for cancers, often with the use of florid testimonials. This information, however, is often less conclusive than it appears, such as reports from patients who were taking fenbendazole alongside conventional drugs, radiation and/or surgery, making it impossible to tell what caused their recovery.[19]

See also

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References

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  1. ^Nguyen J, Nguyen TQ, Han B, Hoang BX (1 September 2024)."Oral Fenbendazole for Cancer Therapy in Humans and Animals".Anticancer Research.44 (9):3725–3735.doi:10.21873/anticanres.17197.ISSN 0250-7005.PMID 39197912.
  2. ^Baksheeva VE, La Rocca R, Allegro D, Derviaux C, Pasquier E, Roche P, et al. (2025)."NanoDSF Screening for Anti-tubulin Agents Uncovers New Structure–Activity Insights".Journal of Medicinal Chemistry.68 (16):17485–17498.doi:10.1021/acs.jmedchem.5c01008.PMC 12406199.PMID 40815226.
  3. ^Duan Q, Liu Y, Rockwell S (February 2013)."Fenbendazole as a potential anticancer drug".Anticancer Research.33 (2):355–362.PMC 3580766.PMID 23393324.
  4. ^Dogra N, Kumar A, Mukhopadhyay T (August 2018)."Fenbendazole acts as a moderate microtubule destabilizing agent and causes cancer cell death by modulating multiple cellular pathways".Scientific Reports.8 (1) 11926.Bibcode:2018NatSR...811926D.doi:10.1038/s41598-018-30158-6.PMC 6085345.PMID 30093705.
  5. ^"Fenbendazole (Panacur®, Safe-guard®) for Dogs and Cats".www.petmd.com. Retrieved2024-07-01.
  6. ^"What Is Fenbendazole and Is FenCare Right for My Horse? | Farnam".www.farnam.com. Retrieved2024-07-01.
  7. ^"Fenbendazole"(PDF).
  8. ^abPlumb DC (2005).Plumb's veterinary drug handbook (Fifth ed.). Stockholm, Wis.: PhrmaVet.ISBN 978-0-8138-0518-4.
  9. ^Sarangi LN, Tharani N, Polapally S, Rana SK, Thodangala N, Bahekar VS, et al. (March 2021)."Infectious bovine abortions: observations from an organized dairy herd".Brazilian Journal of Microbiology.52 (1):439–448.doi:10.1007/s42770-020-00414-x.PMC 7966683.PMID 33415719.
  10. ^Junquera P (2015-07-26)."Fenbendazole, Anthelmintic for Veterinary Use on Cattle, Sheep, Goats, Pig, Poultry, Horses, Dogs and Cats Against Roundworms and Tapeworms".PARASITIPEDIA. Retrieved2015-09-08.
  11. ^Junquera P (2015-07-26)."Oxfendazole, Anthelmintic for Veterinary Use on Cattle, Sheep, Goats, Horses, Dogs and Cats Against Roundworms and Tapeworms".PARASITIPEDIA. Retrieved2015-09-08.
  12. ^Junquera P (2015-07-26)."Febantel for Veterinary Use on Dogs, Cats, Cattle, Sheep, Goats, Pig and Poultry Against Roundworms and Tapeworms".PARASITIPEDIA. Retrieved2015-09-08.
  13. ^"Prescription Label"(PDF). Retrieved1 July 2024.
  14. ^Medicine Cf (2024-04-08)."Dear Veterinarian Letter regarding adverse events associated with extra-label use of fenbendazole in dogs".FDA.
  15. ^Yamaguchi T, Shimizu J, Oya Y, Horio Y, Hida T (2021)."Drug-Induced Liver Injury in a Patient with Nonsmall Cell Lung Cancer after the Self-Administration of Fenbendazole Based on Social Media Information".Case Reports in Oncology.14 (2):886–891.doi:10.1159/000516276.ISSN 1662-6575.PMC 8255718.PMID 34248555.
  16. ^Green A, Henderson P (October 2023)."S3634 Colon Cleanse Revenge Fenbendazole Causes Severe Drug-Induced Liver Injury".American Journal of Gastroenterology.118 (10S): S2360.doi:10.14309/01.ajg.0000964176.99606.b1.
  17. ^Nguyen J, Nguyen TQ, Han BO, Hoang BX (September 2024)."Oral Fenbendazole for Cancer Therapy in Humans and Animals".Anticancer Research.44 (9):3725–3735.doi:10.21873/anticanres.17197.PMID 39197912.
  18. ^Guerini AE, Triggiani L, Maddalo M, Bonù ML, Frassine F, Baiguini A, et al. (August 2019)."Mebendazole as a Candidate for Drug Repurposing in Oncology: An Extensive Review of Current Literature".Cancers.11 (9): 1284.doi:10.3390/cancers11091284.PMC 6769799.PMID 31480477.{{cite journal}}: CS1 maint: overridden setting (link)
  19. ^abGorski D (4 March 2024)."Fenbendazole is fast becoming the laetrile of the 2020s".Science-Based Medicine. Retrieved21 July 2025.
Antiplatyhelmintic agents
Antitrematodals
(schistosomicides)
Bindstubulin
AChE inhibitor
Other/unknown
Anticestodals
(taeniacides)
Bindstubulin
Other/unknown
Antinematodal agents
(including
macrofilaricides)
Bindstubulin
Glutamate-gated chloride channel,GABA receptor
NMDA
Other/unknown
CARTooltip Constitutive androstane receptor
PXRTooltip Pregnane X receptor
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